chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221254844221254845GA45GENIChomozygous109368177
1221255106221255107GA32GENICpossibly homozygous109368179
1221255138221255139GA40GENIChomozygous109368180
1221258695221258696AG24GENIChomozygous108544181
1221260231221260232TC30GENIChomozygous108544187
1221260831221260832CG5GENICheterozygous120812870
1221261019221261020GT20GENIChomozygous108544193
1221261473221261474TC24GENIChomozygous108544195
1221262666221262667CG26GENIChomozygous108544201
1221263247221263248AG33GENIChomozygous109368182
1221263279221263280CT27GENIChomozygous108544206
1221263389221263390TC30GENIChomozygous108544208
1221264513221264514TC32GENIChomozygous108544210
1221265287221265288AG29GENIChomozygous108544216
1221265295221265296AG31GENIChomozygous108544218
1221265801221265802AT14GENIChomozygous108544224
1221266098221266099TC21GENIChomozygous108544226
1221266177221266178TC24GENIChomozygous108544228
1221266365221266366AG31GENIChomozygous108544230
1221266622221266623GA35GENIChomozygous108544232
1221266741221266742CT22GENIChomozygous108544234
1221267053221267054AT21GENIChomozygous109368183
1221268701221268702AG16GENIChomozygous108544238